Institute of Toxicology, Bayer Schering Pharma, Wuppertal, Germany.
J Appl Toxicol. 2012 Jul;32(7):488-504. doi: 10.1002/jat.1668. Epub 2011 Apr 1.
Wistar rats were nose-only exposed to pigment-sized iron oxide dust (Fe(3) O(4) , magnetite) in a subchronic 13-week inhalation study according to the OECD testing guidelines TG#413 and GD#39. A 4 week pilot study with a 6 month post exposure period served as basis for validating the kinetic modeling approaches utilized to design the subchronic study. Kinetic analyses made during this post exposure period demonstrated that a diminution in particle clearance and lung inflammation occurred at cumulative exposure levels exceeding the lung overload threshold. Animals were exposed 6 h per day, five days per week for 13 consecutive weeks at actual concentrations of 0, 4.7, 16.6 and 52.1 mg m(-3) (mass median aerodynamic diameter ≈1.3 μm, geometric standard deviation = 2). The exposure to iron oxide dust was tolerated without mortality, consistent changes in body weights, food and water consumption or systemic toxicity. While general clinical pathology and urinalysis were unobtrusive, hematology revealed changes of unclear toxicological significance (minimally increased differential neutrophil counts in peripheral blood). Elevations of neutrophils in bronchoalveolar lavage (BAL) appeared to be the most sensitive endpoint of study. Histopathology demonstrated responses to particle deposition in the upper respiratory tract (goblet cell hyper- and/or metaplasia, intraepithelial eosinophilic globules in the nasal passages) and the lower respiratory tract (inflammatory changes in the bronchiolo-alveolar region). Consistent changes suggestive of pulmonary inflammation were evidenced by BAL, histopathology, increased lung and lung-associated-lymph node (LALN) weights at 16.6 and 52.1 mg m(-3) . Increased septal collagenous fibers were observed at 52.1 mg m(-3) . Particle translocation into LALN occurred at exposure levels causing pulmonary inflammation. In summary, the retention kinetics iron oxide reflected that of poorly soluble particles. The empirical no-observed-adverse-effect level (NOAEL) and the lower bound 95% confidence limit on the benchmark concentration (BMCL) obtained by benchmark analysis was 4.7 and 4.4 mg m(-3) , respectively, and supports an OEL (time-adjusted chronic occupational exposure level) of 2 mg m(-3) (alveolar fraction).
Wistar 大鼠在亚慢性 13 周吸入研究中,仅通过鼻子暴露于颜料大小的氧化铁粉尘(Fe(3)O(4),磁铁矿)中,该研究符合 OECD 测试指南 TG#413 和 GD#39。一项为期 4 周的试点研究和 6 个月的暴露后阶段为验证用于设计亚慢性研究的动力学建模方法提供了依据。在暴露后阶段进行的动力学分析表明,在累积暴露水平超过肺过载阈值时,颗粒清除率和肺部炎症会减少。动物每天暴露 6 小时,每周暴露 5 天,连续 13 周,实际浓度分别为 0、4.7、16.6 和 52.1mg/m(3)(质量中值空气动力学直径≈1.3μm,几何标准偏差=2)。氧化铁粉尘暴露没有导致死亡率,体重、食物和水的摄入或全身毒性没有发生一致变化。尽管一般临床病理学和尿液分析没有变化,但血液学显示出具有不确定毒性意义的变化(外周血中性粒细胞计数略有增加)。支气管肺泡灌洗液(BAL)中中性粒细胞的升高似乎是研究中最敏感的终点。组织病理学显示对上呼吸道(杯状细胞增生和/或化生,鼻道上皮内嗜酸性球体)和下呼吸道(细支气管肺泡区域的炎症变化)中颗粒沉积的反应。BAL、组织病理学、肺和肺相关淋巴结(LALN)重量的增加以及 16.6 和 52.1mg/m(3) 时的肺部炎症一致变化表明存在肺部炎症。在 52.1mg/m(3) 时观察到隔胶原纤维增加。颗粒向 LALN 的转移发生在引起肺部炎症的暴露水平。总之,氧化铁的保留动力学反映了难溶性颗粒的动力学。通过基准分析获得的经验无观察到不良效应水平(NOAEL)和基准浓度(BMCL)的下限 95%置信限分别为 4.7 和 4.4mg/m(3),支持 OEL(时间调整慢性职业暴露水平)为 2mg/m(3)(肺泡分数)。